2RFR
Crystal structure of an ntf2-like protein with a cystatin-like fold (saro_3722) from novosphingobium aromaticivorans dsm at 1.16 A resolution
Experimental procedure
| Experimental method | MAD |
| Source type | SYNCHROTRON |
| Source details | ALS BEAMLINE 8.2.1 |
| Synchrotron site | ALS |
| Beamline | 8.2.1 |
| Temperature [K] | 100 |
| Detector technology | CCD |
| Collection date | 2007-09-14 |
| Detector | ADSC QUANTUM 315 |
| Wavelength(s) | 0.9797, 1.0000 |
| Spacegroup name | P 3 2 1 |
| Unit cell lengths | 63.135, 63.135, 75.118 |
| Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
| Resolution | 27.338 - 1.160 |
| R-factor | 0.142 |
| Rwork | 0.141 |
| R-free | 0.17200 |
| Structure solution method | MAD |
| RMSD bond length | 0.018 |
| RMSD bond angle | 1.747 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Phasing software | SOLVE |
| Refinement software | REFMAC (5.3.0040) |
Data quality characteristics
| Overall | Inner shell | Outer shell | |
| Low resolution limit [Å] | 27.338 | 27.338 | 1.190 |
| High resolution limit [Å] | 1.160 | 5.190 | 1.160 |
| Rmerge | 0.085 | 0.038 | 0.618 |
| Total number of observations | 3726 | 12790 | |
| Number of reflections | 60052 | ||
| <I/σ(I)> | 5.6 | 15.9 | 1.2 |
| Completeness [%] | 99.5 | 99.2 | 94.4 |
| Redundancy | 4.7 | 4.9 | 3.1 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 6 | 277 | NANODROP, 20.0% PEG 6000, 0.1M MES pH 6.0, VAPOR DIFFUSION, SITTING DROP, temperature 277K |






